“I doubt that the “scientific discovery” of unwarranted and mean-spirited scapegoating of the unvaccinated surprises most of my readers, but the details of the “findings” are interesting.” Igor Reports.
Category: Covid-19 Vaccine
Author of Study Used to Vilify Unvaxed Had Ties to Pfizer — New Peer-Reviewed Research Shows Why the Study Was Flawed
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“A new peer-reviewed study by researchers Joseph Hickey, Ph.D., and Denis Rancourt, Ph.D., re-examined the mathematical models used to justify policies that barred unvaccinated people from public venues. They found the models were based on the application of flawed mathematical risk models.
During the COVID-19 pandemic, politicians, scientists and media organizations vilified unvaccinated people, blaming them for prolonging the pandemic and advocating policies that barred “the unvaccinated” from public venues, businesses and their own workplaces.”
‘No Real Debate’ After New Study Shows mRNA From COVID Shots Contaminates Breast Milk
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This article was originally published by The Defender — Children’s Health Defense’s News & Views Website.
A peer-reviewed study published Sept. 19 in The Lancet provides “pretty conclusive proof” that mRNA from the COVID-19 vaccines migrates into breast milk, according to internet lecturer John Campbell, Ph.D. — despite claims by regulators, public officials and doctors that the mRNA in the vaccine would stay localized at the injection site.
A new peer-reviewed study provides “pretty conclusive proof” that mRNA from the COVID-19 vaccines migrates into breast milk — “probably for the first 48 hours after vaccination,” according to internet lecturer John Campbell, Ph.D.
Campbell, a retired emergency room nurse, teacher and author of two nursing textbooks, reviewed the study, published Sept. 19 in The Lancet, in a video presentation.
According to the study, the breast milk of 10 of 13 women who took the vaccine tested positive for mRNA up to 45 hours after the vaccine was administered.
The study confirmed the transportation of the synthetic mRNA lipid nanoparticles to the mammary glands via the bloodstream or lymphatic system, leading to its presence in breast milk, Campbell said.
“This is consistent with other studies, so there’s no real debate about this anymore,” he added.
The study did not investigate the effects of the contaminated breast milk on infants, Campbell said.
A study last year in JAMA Pediatrics produced similar results.
Regulatory bodies failed to disclose risk
According to Campbell, regulators, public officials and doctors worldwide initially claimed the mRNA in the vaccine would stay localized at the injection site.
For example, mothers were reassured by the Academy of Breastfeeding Medicine (ABM) in a statement released on Dec. 14, 2020, that the vaccine lipid was unlikely to enter the bloodstream and reach breast tissue.
“If it does, it is even less likely that either the intact nanoparticle or mRNA transfer into milk,” the ABM said.
The American College of Obstetrics and Gynecology had — and continues to promote — a similar message.
Referring to the lipid nanoparticles carrying the mRNA, Campbell said, “If these people had gone to the bother of talking to anyone who specializes in pharmacokinetics … they would have said, ‘Well, with this size particle, it’s … almost certain to be distributed everywhere.’”
“It goes to your liver. It goes to your heart,” he said. “In this case, through the breasts. … It probably goes everywhere. It’s a pity we weren’t told.”
Campbell said he was “pretty cross” because such a disclosure would have reversed his decision to get vaccinated.
He pointed out that in the initial trials, breastfeeding mothers, pregnant women and infants were excluded, “yet the regulatory body still decided to go ahead and give these vaccines [to these groups] which weren’t tested.”
“That’s a question they really need to answer,” he said.
mRNA ‘hijack[s] natural process of genetic communication’
Referring to an illustration provided in the study, Campbell said synthetic mRNA can “hijack the natural process of genetic communication.”
He described the mechanism of action this way:
- The synthetic mRNA is packaged into extracellular vesicles (EVs) and secreted into breast milk. EVs are similar to the body’s own lipid nanoparticles that are naturally present in breast milk.
- This process, a natural way for mothers to transfer RNA to their babies, is mimicked by the synthetic mRNA.
- The synthetic mRNA lipid nanoparticles enter mammary epithelial cells responsible for producing milk.
- The mRNA is released into the cytosol (the clear, colloidal area) of these cells and could be packaged into EVs or excreted by various mechanisms such as exosomes, along with breast milk components.
- The EVs do not express the spike protein but serve as carriers for the synthetic mRNA.
- The study found the mRNA in the breast milk was a degraded form with only 12-25% efficiency compared to the original vaccine.
Campbell emphasized that the only way the mRNA could get to the breast tissue would be if it were “systemically absorbed.”
mRNA vaccine manufacturing built on ‘completely flawed’ science
Speaking of other biodistribution studies, Campbell said the lipid nanoparticles could find their way to the myocardium, perhaps the vascular endothelium in the coronary vessels, creating an autoimmune response.
RNA from vaccines can produce antigens that stimulate inflammatory responses from cytotoxic T-cells. Even lipid nanoparticles can potentially cause inflammatory reactions, Campbell said.
The huge mRNA manufacturing efforts “are based on a completely flawed … fundamental scientific problem … until the liquid nanoparticle systemic distribution problem is solved,” Campbell said. “And yet, this massive investment is going ahead, looking to replace the traditional vaccines.”
According to Campbell, pharmaceutical companies are overlooking these problems because they will be able to develop new patentable products that ensure vast new income streams.
He emphasized the need for large-scale epidemiological surveys, conducted by organizations such as the Centers for Disease Control and Prevention and the U.K.’s Medicines and Healthcare products Regulatory Agency, to gather more information about potential risks associated with the systemic distribution of the vaccines.
Campbell discussed the HT-29 cell line, derived from colon cancer tumors, that has been used in vitro since 1964 to study absorption, transport and secretion by intestinal cells.
The study exposed these cells to the mother’s milk, which failed to produce the spike protein. Campbell said this was inconclusive as they mimic only intestinal cells, not all other cells exposed to the mRNA.
Campbell also called for further research on the effect on newborns and for healthcare workers to have candid discussions with lactating mothers before vaccination.
Manufacturers should “give us really good reasons why lipid nanoparticles will not be systemically distributed in their new products,” Campbell said.
“Let us as a human race proceed with humility — although I don’t think there’s much chance of that,” he said.
Watch here:
This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.
45 Deaths, 5,000+ Adverse Events Following Updated Booster Shots Reported to VAERS, CDC Data Show
VAERS data released Friday by the Centers for Disease Control and Prevention show 1,447,520 reports of adverse events from all age groups following COVID-19 vaccines, including 31,696 deaths and 263,462 serious injuries between Dec. 14, 2020, and Oct. 21, 2022.
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This article was originally published by The Defender — Children’s Health Defense’s News & Views Website.
The Centers for Disease Control and Prevention (CDC) today released new data showing a total of 1,447,520 reports of adverse events following COVID-19 vaccines were submitted between Dec. 14, 2020, and Oct. 21, 2022, to the Vaccine Adverse Event Reporting System (VAERS).
VAERS is the primary government-funded system for reporting adverse vaccine reactions in the U.S.
The data included a total of 31,696 reports of deaths and 263,462 serious injuries, including deaths, during the same time period.
There were a total of 5,435 reports of adverse events following the new COVID-19 bivalent booster as of Oct. 21, 2022. The data included a total of 45 deaths and 280 serious injuries. As of Oct. 27, 22.8 million people have received the updated bivalent booster dose.
Of the 31,696 reported deaths, 20,252 cases are attributed to Pfizer’s COVID-19 vaccine, 8,599 cases to Moderna, 2,752 cases to Johnson & Johnson (J&J) and no cases yet reported for Novavax.
Excluding “foreign reports” to VAERS, 887,564 adverse events, including 14,920 deaths and 92,482 serious injuries, were reported in the U.S. between Dec. 14, 2020, and Oct. 21, 2022.
Foreign reports are reports foreign subsidiaries send to U.S. vaccine manufacturers. Under U.S. Food and Drug Administration (FDA) regulations, if a manufacturer is notified of a foreign case report that describes an event that is both serious and does not appear on the product’s labeling, the manufacturer is required to submit the report to VAERS.
Of the 14,920 deaths reported as of Oct. 21, 7% occurred within 24 hours of vaccination and 15% occurred within 48 hours of vaccination.
In the U.S., 632 million COVID-19 vaccine doses had been administered as of Oct. 19, including 376 million doses of Pfizer, 238 million doses of Moderna and 19 million doses of J&J.
Every Friday, VAERS publishes vaccine injury reports received as of a specified date. Reports submitted to VAERS require further investigation before a causal relationship can be confirmed. Historically, VAERS has been shown to report only 1% of actual vaccine adverse events.
VAERS data from Dec. 14, 2020, to Oct. 21, 2022, for 6-month-olds to 5-year-olds show:
- 4,482 adverse events, including 187 cases rated as serious and 8 reported deaths.
- 5 reports of myocarditis and pericarditis (heart inflammation).
The CDC uses a narrowed case definition of “myocarditis,” which excludes cases of cardiac arrest, ischemic strokes and deaths due to heart problems that occur before one has the chance to go to the emergency department. - 27 reports of blood clotting disorders.
- 46 reports of seizures.
VAERS data from Dec. 14, 2020, to Oct. 21, 2022, for 5- to 11-year-olds show:
- 14,938 adverse events, including 701 rated as serious and 29 reported deaths.
- 47 reports of myocarditis and pericarditis.
- 71 reports of blood clotting disorders.
- 183 reports of seizures.
VAERS data from Dec. 14, 2020, to Oct. 21, 2022, for 12- to 17-year-olds show:
- 40,045 adverse events, including 4,358 rated as serious and 129 reported deaths.
According to the CDC, “VAERS data available to the public include only the initial report data to VAERS. Updated data which contains data from medical records and corrections reported during follow up are used by the government for analysis. However, for numerous reasons including data consistency, these amended data are not available to the public.”
- 269 reports of anaphylaxis among 12- to 17-year-olds where the reaction was life-threatening, required treatment or resulted in death.
- 1,336 reports of myocarditis and pericarditis with 1,167 cases attributed to Pfizer’s vaccine.
- 301 reports of blood clotting disorders with 278 cases attributed to Pfizer.
- 27 cases of postural orthostatic tachycardia syndrome (POTS) with all cases attributed to Pfizer’s vaccine.
VAERS data from Dec. 14, 2020, to Oct. 21, 2022, for all age groups combined, show:
- 16% of deaths were related to cardiac disorders.
- 53% of those who died were male, 42% were female and the remaining death reports did not include the gender of the deceased.
- The average age of death was 72.
- As of Oct. 21, 8,608 pregnant women reported adverse events related to COVID-19 vaccines, including 5,027 reports of miscarriage or premature birth.
- Of the 16,555 cases of Bell’s Palsy reported, 73% were attributed to Pfizer vaccinations, 22% to Moderna and 5% to J&J.
- 3,040 reports of Guillain-Barré syndrome.
- 10,100 reports of anaphylaxis where the reaction was life-threatening, required treatment or resulted in death.
- 4,844 reports of myocardial infarction.
- 43,699 reports of blood-clotting disorders. Of those, 29,940 reports were attributed to Pfizer, 9,849 reports to Moderna and 3,820 reports to J&J.
- 24,438 cases of myocarditis and pericarditis with 18,514 cases attributed to Pfizer, 5,459 cases to Moderna and 417 cases to J&J.
- 70 cases of Creutzfeldt-Jakob disease with 57 cases attributed to Pfizer, 12 cases to Moderna and 1 case to J&J.
- 564 cases of POTS with 418 cases attributed to Pfizer, 125 cases to Moderna and 21 cases to J&J.
Children’s Health Defense (CHD) asks anyone who has experienced an adverse reaction, to any vaccine, to file a report following these three steps.
CDC pressured FDA to authorize COVID boosters without clinical trials
The CDC pressured U.S. regulators to clear COVID-19 boosters without clinical trial data, according to emails obtained by Judicial Watch.
CDC officials relayed to counterparts at the FDA in early August 2021 that they wanted authorization for Moderna and Pfizer boosters, as data began showing that the vaccines weren’t working as well as initially promoted.
The conversation took place on a call that was described by Dr. Phil Krause, a top FDA official, to several other FDA workers. On that call, the CDC “evidently stated” they would assemble all the data they were aware of on third dosing in the immunocompromised setting and send it to the FDA in hopes they would authorize a third dose for those with compromised immune systems under Emergency Use Authorization.
All COVID-19 vaccines were authorized only for emergency use at that time. No boosters had been authorized and no clinical data were available for a third vaccine dose. Less than two weeks later, the FDA authorized boosters for certain people, including immunocompromised persons.
The agency said “a thorough review of the available data” concluded the group “may benefit” from a third dose. The only data cited on efficacy were from two studies, one conducted by French researchers and another by Canadian researchers. Pfizer and Moderna hadn’t completed any clinical trials.
FDA slow-walked studies on COVID vaccine safety signals in elderly
The FDA took more than a year to follow up on a potential increase in serious adverse events in elderly people who received Pfizer’s COVID-19 vaccine, according to an investigative report published Tuesday by The BMJ.
According to The BMJ, in July 2021, the FDA “quietly disclosed” the findings of a potential increase in four types of serious adverse events in elderly people who had received a Pfizer COVID-19 vaccine: acute myocardial infarction, disseminated intravascular coagulation, immune thrombocytopenia, and pulmonary embolism.
The FDA disclosure lacked specific details, such as the magnitude of the increased potential risk, and the agency said it would “share further updates and information with the public as they become available.”
The FDA did not alert physicians or the public, via a press release or any other means, The BMJ investigator said.
Eighteen days later, the FDA published a study planning document that outlined a protocol for a follow-up epidemiological study for investigating the matter more thoroughly.
According to the BMJ, the recondite technical document disclosed the unadjusted risk ratio estimates originally found for the four serious adverse events, which ranged from 42% to 91% increased risk.
More than a year later, the status and results of the follow-up study are unknown. The BMJ report also alleged the FDA has not “publicly acknowledged other published observational studies or clinical trial reanalyses reporting compatible results.”
CDC knew COVID shots could cause myocarditis in young males months before telling the public
Two months after COVID-19 vaccines were rolled out to the U.S. public, a statistically significant vaccine safety signal for myocarditis in males ages 8 to 21 appeared in the CDC’s VAERS database, but CDC officials waited another three months before alerting the public, according to a new study.
The study, “Delayed Vigilance: A Comment on Myocarditis in Association with the COVID-19 Injections,” by Karl Jablonowski, Ph.D., and Brian Hooker, Ph.D., P.E., was published on Oct. 17 in the International Journal of Vaccine Theory, Practice, and Research.
In their study, Jablonowski and Hooker recorded and analyzed the increasing incidence of myocarditis as it progressively became a statistically significant “signal” in VAERS.
In an interview with The Defender, Hooker said the paper shows a “strong, statistically significant vaccine adverse event ‘signal’ for myocarditis in males 8 to 21 years of age was seen on the VAERS database as early as Feb. 19, 2021, just two months after the release of the COVID-19 vaccine to the U.S. public.”
Yet, instead of sounding the alarm, “CDC officials buried the connection between COVID-19 vaccination and myocarditis until May 27, 2021,” Hooker added. “By this date, over 50% of the eligible U.S. population had received at least one mRNA COVID-19 vaccine.”
All age groups at higher risk of myocarditis death after COVID vaccines
People of all ages are at higher risk of death from heart inflammation after COVID-19 vaccination compared with the typical occurrence of myocarditis death, according to a new preprint study.
Researchers in Japan analyzed deaths caused by myocarditis, a form of heart inflammation, where the myocarditis set in within 28 days of vaccination. Thirty-eight deaths fit the definition, about half of which were diagnosed by autopsy and or biopsy, with the others being determined through tools such as blood tests and electrocardiograms.
Researchers then took the vaccinated mortality rate and compared it with the death from myocarditis rate from the general population before the pandemic, in the years 2017 to 2019.
Using data provided by the Japanese government, the researchers observed an increased myocarditis mortality rate ratio in the SARS-CoV-2 vaccinated population compared with the general population during the three years pre-COVID-19 pandemic era, especially in young adults.
An increased risk was also observed in the middle-aged (40s) and elderly vaccinated populations.
Even estimating the lowest level of the effect, the risk of COVID-19 vaccination on myocarditis death would be at least four times higher than the unadjusted mortality risk, the researchers said. There are also signs that some post-vaccination deaths aren’t reported properly, they added.
Recent studies identify new concerns related to COVID vaccines and organ transplants
Recent studies identified a new concern related to the failure of transplanted kidneys and other organs: COVID-19 vaccination.
In one study, published in September in Transplant Infectious Disease, researchers cataloged acute organ rejection within a week or two of COVID-19 vaccination in five individuals who had received kidney, liver or heart transplants six to 18 months earlier.
In August, Japanese researchers reported rejection of corneal grafts — which ordinarily have a high success rate — in COVID-19 vaccine recipients, occurring from one day to six weeks post-vaccination.
Noting literature that documents transplant rejection in association with other vaccines such as influenza, hepatitis B, tetanus and yellow fever, the Japanese authors expressed worry about what “the projected societal shift towards a more frequent vaccination schedule” portends for transplant recipients.
Concerns about the impact of COVID-19 jabs on people with existing transplants are important, but another pressing-yet-unaddressed issue is what happens when an unvaccinated person receives a transplanted organ from someone who received a COVID-19 vaccination.
Woman injured by Gardasil vaccine shares how COVID shots injured her mother and ended the life of her grandmother
In 2012, when she was 20 years old, Rochelle was so injured by Merck’s Gardasil vaccine that she had to give up her pre-med studies.
Ten years later, her mother was injured by Moderna’s COVID-19 vaccine, and shortly after, her grandmother died just a few weeks after getting her second dose of Pfizer’s vaccine.
In an exclusive interview with The Defender, Rochelle, now 30, shared her story, and her mother and grandmother’s stories. Rochelle told The Defender that her father, grandfather and brother all became doctors, and her mother, Marcia, was a nurse.
Rochelle’s mother received both doses of the Moderna vaccine in the spring of 2021. Adverse events followed soon after the first dose and she was diagnosed with polymyalgia rheumatica (PMR), which her doctor said was induced by the vaccine.
Marcia’s PMR “caused severe inflammation throughout her body,” leading to “spontaneous tendon ruptures and a lower back disc herniation,” said Rochelle. In addition, “she tore her thumb tendon just by moving her hand normally and required urgent surgery to repair it.”
Rochelle said her mother will need several surgeries for complete tendon tears in her shoulder, and may potentially need spine surgery to repair her herniated disc. She is also on medication and for a long time, could not perform basic tasks.
What happened to Rochelle after getting the Gardasil human papillomavirus, or HPV, vaccine, and her mother, Marcia, after getting the COVID-19 vaccine was bad enough — but not as bad as what happened to Rochelle’s grandmother. After receiving her second Pfizer vaccine, Jean lost her ability to communicate, her health declined severely and within a few weeks, she was dead.
This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.
Even with the Lowest Distribution in 2023, COVID “Vaccines” are Still the Deadliest Vaccines Accounting for 70% of All Vaccine Deaths
by Brian Shilhavy
Editor, Health Impact News
“The distribution of COVID-19 injections has significantly decreased here in 2023, with the fewest amount of children and adults being injected with these bioweapons since they were introduced in December of 2020.
In the two and a half years since the COVID-19 injections were authorized for emergency use by then President Donald Trump, there have been 676,728,782 doses injected into adults and children in the United States, but only 1.4% of those have been injected in Americans so far here in 2023, with a dramatic reduction of those lining up to receive an injection of the bioweapons.”
One-Third of Adults Polled Think COVID Shots Killed Thousands
By Marco Cáceres
“…In the Rasmussen poll, 77 percent of adults who had not been vaccinated for COVID thought it was at least somewhat likely COVID shots had caused a significant number of unexplained deaths. Perhaps more interestingly, 38 percent of adults who had received a COVID shot thought that the shots were at least somewhat likely to have caused many unexplained deaths.4“
Oxford Study Finds Increased COVID Infection Rate Among the COVID Vaccinated
by Natasha Hobley
“Researchers from Oxford University in the United Kingdom published a study in The Lancet finding that those who received two doses of COVID-19 shot were 44 percent more likely to be infected with the SARS-CoV-2 virus than those who were unvaccinated.”
48,817 DEAD and 5,107,883 Injured Following COVID-19 Vaccines in European Database of Adverse Reactions
by Brian Shilhavy
Editor, Health Impact News
“The European (EEA and non-EEA countries) database of suspected drug reaction reports is EudraVigilance, verified by the European Medicines Agency (EMA), and they are now reporting 48,817 fatalities, and 5,107,883 injuries following injections of four experimental COVID-19 shots…”